WormBase Tree Display for Variation: WBVar01435828

WBVar01435828 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01435828
    Other_name: cewivar00373530
      F53A10.2b.1:c.-961-2974C>T
      F53A10.2a.1:c.138-2974C>T
    HGVSg: CHROMOSOME_II:g.1208103C>T
  Sequence_details: SMap: S_parent: Sequence: F53A10
    Flanking_sequences: AAATTTTAACTTGGAAAATTGGTGAAATCT GTTTTCCGGTACAAAAGCTGTTGTCAAGTT
    Mapping_target: F53A10
    Type_of_mutation: Substitution: c t
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006632 From_analysis: WGS_Andersen
      WBStrain00006640 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00022958 From_analysis: WGS_Andersen
      WBStrain00022960 From_analysis: WGS_Andersen
      WBStrain00023079 From_analysis: WGS_Andersen
      WBStrain00023138 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193323890
        dbSNP_ss ss 295499808
    Status: Live
  Affects: Gene: WBGene00018734
    Transcript: F53A10.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F53A10.2b.1:c.-961-2974C>T
        Intron_number: 1/12
      F53A10.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F53A10.2a.1:c.138-2974C>T
        Intron_number: 2/12
  Reference: WBPaper00040707
  Method: WGS_Andersen